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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Mol Psychiatry. 2021 Aug;26(8):4496-4510. doi: 10.1038/s41380-020-0654-3. Epub 2020 Feb 3.
Mol Psychiatry. 2021.
PMID: 32015465
Free PMC article.
[GEITDAH consensus on conduct disorders in children and adolescents].
Sasot-Llevadot J, Ibáñez-Bordas RM, Soto-López A, Montañés-Rada F, Gastaminza-Pérez X, Alda-Díez JA, Cantó-Díez T, Catalá MA, Ferrin-Erdozáin M, García-Giral M, Graell-Bernal M, Granada-Jiménez O, Herreros-Rodríguez Ó, Mardomingo-Sanz MJ, Mojarro-Práxedes D, Morey-Canyelles J, Ortiz-Guerra J, Pàmies-Massana M, Rey-Sánchez F, Romera-Torrens M, Rubio-Morell B, Ruiz-Lázaro PM, Ruiz-Sanz F; Grupo de Especial Interés en el Trastorno por Déficit de Atención/Hiperactividad (GEITDAH).
Sasot-Llevadot J, et al. Among authors: morey canyelles j.
Rev Neurol. 2015 Aug 16;61(4):167-82.
Rev Neurol. 2015.
PMID: 26204088
Free article.
Spanish.
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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, van Amelsvoort T, Arango C, Armando M, Campbell LE, Cubells JF, Eliez S, Garcia-Minaur S, Gothelf D, Kates WR, Murphy KC, Murphy CM, Murphy DG, Philip N, Repetto GM, Shashi V, Simon TJ, Suñer DH, Vicari S, Scherer SW; International 22q11.2 Brain and Behavior Consortium; Bearden CE, Vorstman JAS.
Davies RW, et al.
Nat Med. 2020 Dec;26(12):1912-1918. doi: 10.1038/s41591-020-1103-1. Epub 2020 Nov 9.
Nat Med. 2020.
PMID: 33169016
Free PMC article.
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